Phase 2 Pancreatic Cancer Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People with locally advanced pancreatic cancer that cannot be removed by surgery, confirmed by a tissue or cell sample test, as classified by a standard medical staging system
- People aged between 18 and 80 years
- People who have at least one pancreatic cancer lesion that can be measured using standard imaging criteria
- People with a good general level of physical functioning, rated 0 or 1 on a standard medical scale (meaning able to carry out normal daily activities with little or no restriction)
- People with a life expectancy of at least 3 months
- People whose blood counts, kidney function, and liver function fall within acceptable ranges on tests taken within 14 days before joining (confirm specific values with trial site)
- People who are able to provide tissue and blood samples for research purposes
- People who are able to understand the study details and sign a written consent form
Who may not be able to join:
- People who have had any other cancer in the past 5 years, except for certain localised cancers that have been fully treated and cured
- People with uncontrolled infections (such as active tuberculosis or hepatitis), uncontrolled whole-body illnesses, poorly controlled high blood pressure or diabetes, or serious health events in the past 6 months such as a heart attack, stroke, or significant heart rhythm problems
- People who have previously been treated with certain drugs that target specific parts of the immune system's T-cell response (confirm with trial site)
- People who have received radiation therapy within 2 weeks before joining the trial
- People with a known allergy to the study drug Ivonescimab or any of its ingredients
- People who are pregnant or currently breastfeeding
- People who are currently using or planning to use certain medications that strongly affect how the body processes drugs (known as strong CYP3A4/5 or CYP1A2 inducers or inhibitors — confirm specific medications with trial site)
- People who require certain blood-thinning tablets called oral vitamin K antagonists (such as full-dose warfarin), though low-dose warfarin and some other low-dose blood thinners may be permitted (confirm with trial site)
- People who have conditions that affect their ability to take oral medications, including a history of a hole or abnormal opening in the gut in the past 6 months, bowel obstruction, large bowel surgery, Crohn's disease, ulcerative colitis, or ongoing chronic diarrhoea
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Jinbo Yue, Doctor, Shandong Cancer Hospital and Institute
Phone: 0531-67626442
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Maximum Tolerated Dose (MTD); Dose-Limiting Toxicity (DLT); Recommended Phase 2 Dose (RP2D); Progression-Free Survival (PFS)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 23 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.